GUDIDData
gudid Primary ID: TR700-10210

CORITON (UDI TR700-10210)

Manufactured by CORITON Instrument Co.,Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CORITON - Primary ID TR700-10210

Device Regulatory Overview

The CORITON (Model/Catalog Number: TR700-10210) is a medical device manufactured by CORITON Instrument Co.,Ltd. This product is indexed under FDA Product Code / Category Classification FOX within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
TR700-10210
Product Code / EMDN
FOX
Device Name
Trolley for Medical Device,Height Adjustable
Database Sync Date
2026-08-09 09:06:39

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of CORITON?

The registered manufacturer of record for CORITON is CORITON Instrument Co.,Ltd.

What is the Primary UDI-DI identifier for CORITON?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is TR700-10210.

What classification code is assigned to this device?

This device is registered under product classification code FOX.

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